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EUDAMED last updated this device on Dec 12, 2023
871887331701M5PO 31701 M is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Lomed Nederland. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08718873001018871887331701M5PO 31701 M(01)08718873001018
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Y061209KNEE ORTHOSESNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Netherlands; available across 1 country total.
Placed on the market in Netherlands; per-country availability dates not published.
NL-MF-000032807No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.